This is your event if you want to understand what is up to you regarding the mandatory labelling requirements for UAE market! The UAE’s Ministry of Health and Prevention – MoHAP has published legislation that defines the Serialization and Track & Trace (T&T) requirements for all...
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This is your event if you want to understand what is up to you regarding the mandatory labeling requirements for Uzbekistan market! Resolution No. 149 of the Cabinet of Ministers of the Republic of Uzbekistan dated April 2, 2022 “On the introduction of a system of...
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This is your event if you want to understand what is up to you regarding the food supplements serialization! A large range of industries already met the serialization or are in process of developing traceability systems. The Food Supplements Industry is facing the serialization requirements now...
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This is your event if you want to discover the solution covering all MDR requirements! Medical Devices Regulation (MDR) has been fully applicable since the mid of 2021, and every medical device manufacturer have to face new challenges >> Traceability of Medical Devices: The solution to the...
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If you want to learn in details and understand the new Track & Trace requirements regarding medical devices - this is your event! Medical Devices Regulation (MDR) is a real hot topic amongst the supply chain participants. It completely changes the legislation and business processes regarding...
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If you want to learn in details and understand the Track & Trace world, this is your event! The online event was with educational focus and met the attendees with the end-to-end traceability technology in real production. The video materials provided all information about traceability systems –...
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Learn more about the benefits of GS1 Standards, serialization and aggregation Description Discover how the pharma CMO Dovema has answered the track and trace requirements in European and Russian markets thanks to GS1 Standards. We are pleased to invite you to an online training seminar where you have...
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Discover what every aspect of the new EU regulation regarding medical devices stand for! Description The deadline for the introduction of serialization for medical devices and in vitro diagnostic devices is approaching. However, their implementation raises certain questions and challenges for manufacturers, importers, and authorized distributors. We are...
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Learn how to protect your production efficiency Many players in the pharmaceutical industry have been feeling the pain of serialization solutions that are not their “cup of tea”. SoftGroup often hears from your peers about these struggles: overpromised and underdelivered capabilities, high rates of unexpected issues and...
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Learn everything you always wanted to know about printing technology, printers, and printing cartridges A problem with the supplementing equipment in pharmaceutical manufacturing can sometimes be the tip of the iceberg. With more than a year after the Falsified Medicines Directive came effective in Europe and many...
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Learn how the new serialization requirements in Russia will affect the manufacturing and be prepared! In the last years, the serialization landscape has undergone an overall change, with a huge count of new regulations coming into force. It's not a secret that the implementation of the...
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Parallel Importers under the EU FMD It’s been one year since the European Union adopted the Falsified Medicines Directive as a means of combatting counterfeiting in the pharmaceutical industry. What has changed after EU FMD for the Parallel Traders? In this webinar, SoftGroup's Track & Trace experts...
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